Wetting resistant materials and articles made therewith

ABSTRACT

Ceramic materials with relatively high resistance to wetting by various liquids, such as water, are presented, along with articles made with these materials. The oxide materials described herein as a class typically contain one or more of ytterbia (Yb 2 O 3 ) and europia (Eu 2 O 3 ). The oxides may further contain other additives, such as oxides of gadolinium (Gd), samarium (Sm), dysprosium (Dy), or terbium (Tb). In certain embodiments the oxide, in addition to the ytterbia and/or europia, further comprises lanthanum (La), praseodymium (Pr), or neodymium (Nd).

This Application claims priority to U.S. Provisional Patent ApplicationSer. No. 61/122,756, filed Dec. 16, 2008.

This invention was made with Government support under contract number70NANB7H7009, awarded by National Institute of Standards and Technology.The Government has certain rights in the invention.

BACKGROUND

This invention relates to wetting resistant materials. Moreparticularly, this invention relates to articles that include coatingsof wetting resistant materials.

The “liquid wettability”, or “wettability,” of a solid surface isdetermined by observing the nature of the interaction occurring betweenthe surface and a drop of a given liquid disposed on the surface. A highdegree of wetting results in a relatively low solid-liquid contact angleand large areas of liquid-solid contact; this state is desirable inapplications where a considerable amount of interaction between the twosurfaces is beneficial, such as, for example, adhesive and coatingapplications. By way of example, so-called “hydrophilic” materials haverelatively high wettability in the presence of water, resulting in ahigh degree of “sheeting” of the water over the solid surface.Conversely, for applications requiring low solid-liquid interaction, thewettability is generally kept as low as possible in order to promote theformation of liquid drops having high contact angle and thus minimalcontact area with the solid surface. “Hydrophobic” materials haverelatively low water wettability (contact angle generally at or above 90degrees); so-called “superhydrophobic” materials (often described ashaving a contact angle greater than 120 degrees) have even lower waterwettability, where the liquid forms nearly spherical drops that in manycases easily roll off of the surface at the slightest disturbance.

Heat transfer equipment, such as condensers, provide one example of anapplication where the maintenance of surface water as droplets ratherthan as a film is important. Two alternate mechanisms may govern acondensation process. In most cases, the condensing liquid(“condensate”) forms a film covering the entire surface; this mechanismis known as filmwise condensation. The film provides a considerableresistance to heat transfer between the vapor and the surface, and thisresistance increases as the film thickness increases. In other cases,the condensate forms as drops on the surface, which grow on the surface,coalesce with other drops, and are shed from the surface under theaction of gravity or aerodynamic forces, leaving freshly exposed surfaceupon which new drops may form. This so-called “dropwise” condensationresults in considerably higher heat transfer rates than filmwisecondensation, but dropwise condensation is generally an unstablecondition that often becomes replaced by filmwise condensation overtime. Efforts to stabilize and promote dropwise condensation overfilmwise condensation as a heat transfer mechanism in practical systemshave often required the incorporation of additives to the condensingmedium to reduce the tendency of the condensate to wet (i.e., form afilm on) the surface, or the use of low-surface energy polymer filmsapplied to the surface to reduce film formation. These approaches havedrawbacks in that the use of additives may not be practical in manyapplications, and the use of polymer films may insert significantthermal resistance between the surface and the vapor. Polymer films mayalso suffer from low adhesion and durability in many aggressiveindustrial environments.

Texturing or roughening the surface can change the contact angle ofwater on a surface. A texture that increases the tortuosity of thesurface but maintains the contact between water droplet and the surfacewill increase the contact angle of a hydrophobic material and decreasethe contact angel of a hydrophilic material. In contrast, if a textureis imparted that maintains regions of air beneath a water droplet, thesurface will become more hydrophobic. Even an intrinsically hydrophilicsurface can exhibit hydrophobic behavior if the surface is textured tomaintain a sufficiently high fraction of air beneath the water drop.However, for applications requiring highly hydrophobic orsuperhydrophobic behavior, it is generally more desirable in practice totexture a hydrophobic surface than to texture a hydrophilic surface. Anintrinsically hydrophobic surface usually provides the potential for ahigher effective contact angle after texturing than an intrinsicallyhydrophilic surface, and generally provides for a higher level ofwetting resistance even if the surface texturing becomes less effectiveover time as the texture wears away.

Relatively little is known about the intrinsic hydrophobicity of broadclasses of materials. In general, most of the materials known to have acontact angle with water of greater than 90 degrees are polymers such astetrafluoroethylene, silanes, waxes, polyethylene, and propylene.Unfortunately, polymers have limitations in temperature and durabilitythat can limit their application, because many practical surfaces thatwould benefit from low wettability properties are subject in service tohigh temperatures, erosion, or harsh chemicals.

Ceramic materials are typically superior to polymers in many aspectsrelated to durability. Of the ceramic materials, oxide ceramics areparticularly useful because they are highly manufacturable, often havehigh environmental resistance, and can have good mechanical properties.Unfortunately, there are virtually no known oxide ceramics that arehydrophobic. A notable exception is silicalite, a zeolitic polymorph ofSiO2 [E. M. Flanigen, J. M. Bennett, R. W. Grose, J. P. Cohen, R. L.Patton, R. M. Kirchner, and J. V. Smith, “Silicalite, a new hydrophobiccrystalline silica molecular sieve,” Nature, v. 271, 512 (1978)]. Forthat material the specific crystal structure is highly important becauseamorphous SiO2 has a very low, hydrophilic wetting angle. However, thesynthesis conditions required to form zeolite crystals can limit therange of applicability of those materials as hydrophobic surfaces andthe porosity of zeolite crystals makes them less desirable forapplications requiring durability.

Therefore, there remains a need in the art for oxide ceramics that havelower liquid wettability than conventional oxides, promote stabledropwise condensation, are stable at elevated temperatures, are amenableto coating processing, and have good mechanical properties. There isalso a need for articles coated with these wetting resistant oxideceramics.

BRIEF DESCRIPTION

Embodiments of the present invention are provided to meet these andother needs. One embodiment is an article comprising a coating disposedon a substrate, wherein the coating comprises an oxide. The oxide has upto about 25 atomic percent of its total cation content as tetravalentcations. The oxide has a composition defined by the chemical formula(A_(x)B_(1-x))₂O₃; where A comprises Yb or Eu, and B comprises Gd, Sm,Dy, or Tb; and x is in the range from about 0.01 to about 0.99. In thisembodiment, the above is, however, subject to the following: (a)provided that, where A consists essentially of Yb, B consistsessentially of Gd; and (b) provided that, where A consists essentiallyof Eu and B comprises Sm, Dy, or Tb, x is in the range from about 0.5 toabout 0.99.

Another embodiment is an article comprising a coating disposed on asubstrate, wherein the coating comprises an oxide, the oxide having acomposition defined by the chemical formula (Yb_(x)Eu_(1-x))₂O₃; whereinx is in the range from about 0.01 to about 0.99.

Another embodiment is an article comprising a surface situated to beroutinely exposed to a liquid phase, wherein the surface comprises anA₂O₃-type oxide selected from the group consisting of ytterbium oxideand europium oxide.

Another embodiment is a material comprising an oxide comprising fromabout 60 mole % to about 95 mole % gadolinia and at least about 1 mole %ytterbia or europia, wherein the oxide is B-type monoclinic, and whereinthe oxide has up to about 25 atomic percent of its total cation contentas tetravalent cations.

Another embodiment is a material comprising: an oxide comprising atleast about 50 mole % europia; and samaria, terbia, or dysprosia;wherein the material contains up to about 25 atom % of tetravalentcations relative to the total amount of cations present in the material.

Another embodiment is a material comprising: a B-type monoclinic oxidecomprising ytterbia and europia; wherein the oxide contains up to about25 atom % of tetravalent cations relative to the total amount of cationspresent in the material.

Another embodiment is an article comprising: a coating disposed on asubstrate, the coating having a surface connected porosity content of upto about 5 percent by volume, wherein the coating comprises a materialcomprising at least about 20 atom % of a first oxide selected from thegroup consisting of ytterbia, europia, and combinations of these; and asecond oxide selected from the group consisting of lanthana,praseodymia, and neodymia.

DRAWINGS

These and other features, aspects, and advantages of the presentinvention will become better understood when the following detaileddescription is read with reference to the accompanying drawings in whichlike characters represent like parts throughout the drawings, wherein:

FIG. 1 is a schematic cross-section of an article in accordance with oneembodiment of the present invention;

FIG. 2 is a schematic cross-section of an article in accordance withanother embodiment of the present invention; and

FIGS. 3-6 are data plots of water contact angle as a function ofcomposition for various materials as described herein.

DETAILED DESCRIPTION

Embodiments of the present invention are based upon the discovery by theinventors of a class of oxide ceramics that shows certain surprisingproperties. First, they tend to have significantly lower waterwettability than commonly known engineering oxides. Some compositionsare intrinsically hydrophobic. Moreover, some compositions, even thosenot intrinsically hydrophobic, have demonstrated the ability to maintainstable dropwise water condensation, making them intriguing candidatesfor use in heat transfer applications, for instance. Without being boundby theory, it is suspected that this behavior is related to the natureof the oxygen-cation bonding occurring within the crystal structure ofthe oxide. Finally, certain compositions are transparent to ultraviolet,visible, or infrared radiation, meaning they allow at least about 70% ofthe incident radiation to transmit through the material. Suchcompositions may allow for wetting-resistant windows and other usefulapplications, as will be discussed further herein.

Embodiments of the present invention include certain materialcompositions. Other embodiments include coatings and articles thatinclude these compositions. These compositions may exist in any form,such as, for example, powders, coatings, and ingots. The materialsdescribed herein may be a mixture or a compound of multiple oxides.Throughout this description, the composition of the material may bedescribed in terms of its component oxides, such as, for example,gadolinia and europia, even if these component oxides are technicallynot present in the material due to interactions such as phasetransformations and chemical reactions. This notation is consistent withthat commonly used in the art, where, for example, a compound such asytterbium europium oxide may be interchangeably denoted as Yb₂O₃.Eu₂O₃,YbO_(1.5).EuO_(1.5), or YbEuO₃.

It will be appreciated that where materials and articles are describedherein as “comprising” or “including” one or more components, the scopeof the description includes, without limitation, materials made only ofthe stated components; materials made of the stated components andincluding other components that do not materially affect the wettabilityof the material; and materials including the stated components but notexcluding other components. Moreover, where lists of alternatives areprovided, the alternatives are not meant to be exclusive; one or more ofthe alternatives may be selected, except where otherwise explicitlystated.

The oxide materials described herein as a class typically contain one ormore of ytterbia (Yb₂O₃) and europia (Eu₂O₃). The oxides may furthercontain other additives, such as oxides of gadolinium (Gd), samarium(Sm), dysprosium (Dy), or terbium (Tb). In certain embodiments theoxide, in addition to the ytterbia and/or europia, further compriseslanthanum (La), praseodymium (Pr), or neodymium (Nd).

Both ytterbium (III) oxide and europium (III) oxide, which are A₂O₃-typeoxides, have been found to promote dropwise condensation and to beintrinsically hydrophobic. Moreover, combinations (such as solidsolutions) of these two oxides also were shown to have this sameremarkable combination of properties. In one embodiment, mixedytterbium-europium oxides are provided. The oxide has a formula of(Yb_(x)Eu_(1-x))₂O₃; wherein x is in the range from about 0.01 to about0.99. In a particular embodiment, a material comprises a B-typemonoclinic oxide comprising ytterbia and europia, where up to about 25atom percent of the total cations present in the oxide are tetravalentcations. As used herein, “B-type monoclinic” refers to thecrystallographic structure known in the art as 2 C/m to refer to certainrare earth oxides. (Handbook on the Physics and Chemistry of RareEarths, volume 3. Editors: K A Gschneidner and L Eyring, pp 349ff.Elsevier Science Publishers, New York, N.Y. 1979.) The B-type monoclinicoxides described herein tend to show very desirable hydrophobicity andpromotion of dropwise condensation. It was also found in some instancesthat having a high amount of tetravalent cations present in the materialdetracted from its wettability and condensation properties. In someembodiments, this B-type oxide further comprises an additional materialsuch as Sm, Dy, or Tb, and in particular embodiments this additionalmaterial is up to about 50 mole percent of the oxide.

In one embodiment, the oxide of the present invention has a compositiondefined by the chemical formula (A_(x)B_(1-x))₂O₃. Here A comprises Ybor Eu and B comprises Gd, Sm, Dy, or Tb, and x is in the range fromabout 0.01 to about 0.99. In particular embodiments, less than about 25atomic percent of the total cations present in the oxide aretetravalent. Generally these materials have exhibited surprisinglydesirable wettability and condensation properties, but certaincompositions are typically less desirable because poor behavior isobserved or expected. For instance, where A is essentially Yb (i.e., Eucontent is very close to zero save for incidental impurity levels), onlymaterial having B consisting essentially of Gd is expected to show thedesired properties; in some embodiments x is up to about 0.3. Similarly,where A is essentially Eu, levels of Sm, Dy, and/or Tb as denoted by xin the above formula in the range from about 0.5 to about 0.99 mayresult in desirable properties.

One example of a suitable material of the type presented herein, amaterial having attractive wetting and condensation-promotingproperties, comprises an oxide comprising from about 60 mole percent toabout 95 mole percent gadolinia and at least about 1 mole percentytterbia or europia. In accordance with this embodiment, the oxide isB-type monoclinic, and less than about 25 atomic percent of the totalcations present in the oxide are tetravalent. In some embodiments, theoxide comprises up to about 30 mole percent ytterbia, and in certainembodiments the oxide concurrently comprises at least about 70 molepercent gadolinia. In other embodiments, the oxide comprises up to about25 mole percent europia, and may concurrently comprise at least about 75mole percent gadolinia. These embodiments may include “binary” oxides,in which the oxide consists essentially of gadolinia and either ytterbiaor europia but not both; in other embodiments, the oxide comprises bothytterbia and europia in addition to the gadolinia. In certainembodiments, the total amount of ytterbia plus europia present in theoxide is below about 40 mole percent, which provides an oxide that hasshown particularly desirable wettability and condensationcharacteristics.

Certain compositions based on europia are suitable as well. In oneembodiment, the material includes an oxide comprising at least about 50mole percent europia and further comprising samaria, terbia, ordysprosia. Less than about 25 atomic percent of the total cationspresent in the oxide are tetravalent. In certain embodiments, the oxideis B-type monoclinic.

Certain combinations of cations in the above (A_(x)B_(1-x))₂O₃ materialhave shown or are expected to show particularly attractive wettabilityand condensation behavior. In one example, A comprises Eu, such as whereA comprises Eu and B comprises Gd. In a particular embodiment Acomprises Eu and B comprises Gd, and x is in the range from about 0.01to about 0.4, a range which showed particularly good wettabilitybehavior (the contact angle with water measured greater than 100 degreesfor x equal to about 0.2, for instance). Another particular range ofinterest in this system is where x is in the range from about 0.7 toabout 0.9, where contact angle of about 100 degrees was also observed.Where A comprises both Eu and Yb, B, in some embodiments, comprises Gd.In particular embodiments of this type, x is in the range from about0.01 to about 0.3. Alternatively, x may be in the range from about 0.5to about 0.99.

As mentioned above, in certain alternative embodiments the ytterbiumand/or europium oxide material includes one or more of lanthanum (La),praseodymium (Pr), and neodymium (Nd). The present inventors havediscovered that, remarkably, alloying oxides of ytterbium or europiumwith the hydrophobic but normally hygroscopic oxides of La, Pr, or Ndstabilizes these hygroscopic materials in the presence of water andproduces oxides that promote stable dropwise condensation, even thoughthese resultant materials tend to be hydrophilic.

The materials provided in accordance with these embodiments generallycomprise at least about 20 mole percent of a first oxide that isytterbia, europia, or a combination of these, and a second oxide that isan oxide of La, Pr, or Nd. In certain embodiments, the oxide material isdefined by the chemical formula ((A)_(x)B_(1-x))₂O₃, where A is Yb, Eu,or combinations thereof, and B is La, Pr, or Nd. In some embodiments,where B is La or Pr, x is in the range from greater than 0.5 to about0.99. In other embodiments, where B is Nd, x is in the range from about0.2 to about 0.99. Materials in these ranges may exhibit remarkablestability in the presence of water and promote dropwise condensation.

In another embodiment, a material includes a primary oxide comprising aprimary oxide cation of cerium or hafnium. In some embodiments, themolar ratio of the primary oxide cations to total cations present in thematerial is within any of the corresponding ranges provided for thepreviously described material. The material further includes a secondaryoxide that includes (i) a first secondary oxide cation comprisingpraseodymium or ytterbium, and (ii) a second secondary oxide cation thatcomprises a rare earth element, yttrium, or scandium. In certainembodiments, a molar ratio of first secondary oxide cations to totalsecondary oxide cations is in the range from about 0.01 to about 0.99;in certain embodiments this range is from about 0.05 to about 0.95; andin particular embodiments this range is from about 0.1 to about 0.90. Inspecific embodiments, the secondary oxide comprises praseodymium andlanthanum, and in some embodiments the secondary oxide comprisesytterbium and lanthanum.

Further embodiments of the present invention, as illustrated in FIG. 1,include an article 100 comprising a coating 102, where the coating 102comprises any of the materials described herein. In some embodiments,this oxide material (“the material”) makes up greater than about 50percent of the coating volume. In certain embodiments, the materialmakes up greater than about 75 percent of the coating volume, and insome embodiments the material makes up substantially all of the coatingvolume (save for incidental impurities and void space). In someembodiments, this coating 102 has a low level of surface connectedporosity, such as up to about 5 percent by volume. In certainembodiments, the surface connected porosity is even lower, such as lowerthan 2 percent, lower than 1 percent, lower than 0.5 percent, or lowerthan 0.1 percent (all percentages by volume). In some embodiments, thecoating 102 is made of material that is substantially theoreticallydense. A low content of surface connected porosity may inhibit theabsorption of water into a pore network, thereby keeping liquid at thesurface of the article. Even a surface made of highly hydrophobicmaterial, for instance, may absorb water if the amount of open porosityis unduly high, thereby rendering the surface ineffective as a barrierto water.

In some embodiments, the article described above further comprises asubstrate 104, such as a metal substrate, for example, upon which theaforementioned coating 102 is disposed. Examples of metal substratesinclude metals and alloys made with aluminum, steel, stainless steel,nickel, copper, or titanium. In particular, common engineering alloyssuch as 306 stainless steel, 316 stainless steel, 403 stainless steel,422 stainless steel, Custom 450 stainless steel, commercially puretitanium, Ti-4V-6Al, and 70Cu-30Ni are suitable substrates.

Various intermediate coatings (not shown) may be applied for any reason,such as to achieve desired levels of adhesion between substrate andcoating, depending on the nature of the materials involved and theselected methods for processing the materials. Such variations generallyare within the knowledge of one skilled in the art. Thickness of thecoating will depend upon the nature of the environment and theapplication envisioned for the article. For example, in a heat exchangerapplication, the coating is typically designed to minimize thermalresistance between the environment and the substrate while achieving apractical service lifetime. Determination of the coating thickness for agiven application is within the knowledge of one skilled in the art.

In some embodiments the material, whether embodied in a coating orfreestanding object, has a low level of overall porosity, such as lowerthan about 5 percent by volume. In certain embodiments, the overallporosity of the material is even lower, such as lower than about 1percent. In some embodiments, the material is substantiallytheoretically dense throughout. The overall porosity of the material,like the thickness of the coating described above, plays a role indetermining the thermal resistance of the article: higher porositytypically results in high thermal resistance. Thus, maintaining a lowoverall porosity may be important in embodiments where low thermalresistance is desirable.

Any manufacturing method useful for fabrication and/or deposition ofceramic oxide materials may be used for fabricating the materials andarticles described herein. Accordingly, embodiments of the presentinvention include a method for protecting an article from aliquid-containing environment, comprising applying a coating 102 to asubstrate 104, where the coating 102 comprises any of the materialsdescribed herein. Examples of well-known processes capable of makingceramic oxide materials include powder processing, sol-gel processing,chemical vapor deposition and physical vapor deposition. In powderprocessing methods, a ceramic article is formed from ceramic particlesusing a method such as pressing, tape casting, tape calendaring orscreen printing, and then consolidating and densifying the powders usinga sintering process. Sol-gel processing methods provide a ceramicprecursor in liquid form to a substrate after which the ceramic materialis substantially formed through chemical reactions such ashyrdrolyzation and polymerization, and subsequently heat treated toproduce and densify the ceramic material. Chemical vapor depositionmethods involve providing gaseous precursor molecules to a heatedsubstrate to form a ceramic article and include atmospheric pressurechemical vapor deposition, low-pressure chemical vapor deposition,metal-organic chemical vapor deposition and plasma enhanced chemicalvapor deposition. Physical vapor deposition processes produce a vapor ofmaterial from solid precursors and supply the vapor to a substrate toform a ceramic article. Physical vapor deposition processes includesputtering, evaporation, and laser deposition. In the case of bulkceramic articles, the substrate is used to form the ceramic body in theform of a crucible, die or mandrel and subsequently removed. In the caseof ceramic coatings, the ceramic article remains attached to thesubstrate. The processing methods can be selected and tailored by apractitioner skilled in the art to produce the desired control ofchemical composition and density of the ceramic oxide articles.

In some embodiments, the surface of the material, e.g. a coating 102,further comprises a surface texture 106 to further improve thewetting-resistant properties of the article. A surface texture 106comprises features 108 disposed at the surface; examples of suchfeatures include, without limitation, elevations (such as cylindricalposts, rectangular prisms, pyramidal prisms, dendrites, nanorods,nanotubes, particle fragments, abrasion marks, and the like); anddepressions (such as holes, wells, and the like). In some embodiments,the surface texture serves to increase the tortuosity of the surface,which increases the contact angle of a hydrophobic material. In otherembodiments, the features are sized and configured to create pockets ofair between a drop of liquid and the surface, which can reduce theeffective surface energy and produce a higher contact angle than wouldbe expected for a smooth surface. Examples of such textures and methodsfor generating them are described in commonly owned U.S. patentapplication Ser. Nos. 11/497,096; 11/487,023; and 11/497,720; which areincorporated by reference herein in their entireties.

One particular exemplary embodiment of the present invention is awetting-resistant article 100. Article 100 comprises a surface 200situated to be routinely exposed to a liquid phase, meaning that thesurface 200 is positioned in/on the article 100 such that, during normaloperation or maintenance of the article 100, the surface 200 is likelyto come into contact with a liquid phase such as water via anymechanism, including, as examples, condensation or impact. Examples ofsuch articles include condensers, windows, steam turbine blades, or anycomponent commonly exposed to moisture or humidity during operation orservice. Surface 200 comprises any material described herein, such as anA₂O₃-type oxide selected from the group consisting of ytterbium oxideand europium oxide. As illustrated in FIG. 1, surface 200 may bedisposed as part of a coating 102, but this is not necessarily the case;surface 200 may be part of a monolith of the material. In someembodiments, the oxide is present over at least about 50% of the area ofsurface 200; in particular embodiments this area fraction is evenhigher, such as greater than about 75%, and in further embodiments thesurface consists essentially of the oxide.

Thermal barrier coatings made of rare-earth oxide-containingperovskites, such as lanthanum ytterbium oxide (LaYbO₃) are known in theart. See, for example, U.S. Pat. No. 6,821,656. Although thecompositions used for these coatings are similar to some of thosedescribed above, the coatings described in the art have markedlydifferent wetting resistance properties compared to the materials andarticles described herein. Thermal barrier coatings are generallyapplied using thermal spray techniques or physical vapor techniques,both of which are known to produce coatings having relatively highlevels of porosity. Typical industrial thermal barrier coatings haveporosity in the range from about 10 percent to about 25 percent. Theporosity is generally thought to provide an advantage in theseapplications in that it may enhance the thermal resistance and straincompliance of the coating. For instance, it is well documented that thestrain compliance necessary for thermal cycling of thermal barriercoatings requires significant amounts of porosity to be incorporatedinto the coatings, in the form of intercolumnar gaps in EB-PVD coatingsand porosity between splats in thermal spray coatings. The distributionand morphology of coatings deposited by both processes has been studiedextensively to understand the enhancement in thermal resistance in thecoatings as well as the detrimental effects on thermal and mechanicalproperties caused by the sintering loss of the porosity. Such work hasdetermined that sintering of the coating results in a decrease inporosity and increase in Young's modulus, thereby resulting in higherthermally induced stresses and a decrease in thermal fatigue lifetime ofthe thermal barrier coating. For these reasons, thermal barrier coatingsgenerally are structured to maintain a high level of porosity over longlifetimes at elevated temperatures.

In stark contrast to thermal barrier coatings, however, the oxidesapplied in certain embodiments of the present invention aresignificantly denser, because their primary function is not to inhibitheat transfer to the substrate, but to inhibit buildup of liquids, ice,or other foreign matter at the coating surface. The high porosity levelsdescribed in the thermal barrier coating arts generally would not besuitable for use in many embodiments of the present invention. In fact,as noted above, in many heat transfer applications the material isdesigned to minimize thermal resistance, which typically would requireachieving porosity levels that are as low as practically attainable.

The novel properties described for the above embodiments lend themselvesto a host of useful applications where resistance to wetting by liquidsis desirable. A condenser used, for instance, to transfer heat between ahot vapor and a cooling fluid, such as is used in chemical processing,water desalination, and power generation, is an example of an embodimentof the present invention using the articles and materials describedabove. FIG. 2 illustrates one common type of condenser: the surfacecondenser 500. Steam, for example, enters shell 502 through inlet 504,whereupon it is condensed to water on the exterior surface ofcondensation tubes 506, through which flows a cooling fluid 508, such aswater. The material (not shown) described above is disposed on thisexterior surface of the condensation tubes 506, thereby promotingdropwise condensation of condensate water from the steam. The condensateis easily shed from the tubes 506 by the material and exits from shell502 via condensate outlet 510.

In certain applications, such as, for example, steam turbines, metalcomponents are subject to impinging drops of water as well as condensingdrops. As steam expands in a turbine, water droplets (typicallyfog-sized) appear in the flow stream. These droplets agglomerate on theturbine blades and other components and shed off as larger drops thatcan cause thermodynamic, aerodynamic, and erosion losses in turbines.The ability to shed water droplets from components before they have achance to agglomerate into substantially larger drops is thus importantto maximize system lifetime and operation efficiency. As noted above,many of the compositions applied in embodiments of the present inventionpromote dropwise condensation, so that liquid is shed from the surfacein small drops rather than in larger sheets. Accordingly, embodiments ofthe present invention include a steam turbine assembly comprising thearticle described above. In particular embodiments, the article is acomponent of a steam turbine assembly, such as a turbine blade, aturbine vane, or other component susceptible to impingement of waterdroplets during turbine operation.

Certain embodiments of the present invention may reduce the formation,adhesion, and/or accumulation of ice on surfaces. Icing takes place whena water droplet (sometimes supercooled) impinges upon the surface of anarticle, such as an aircraft component or a component of a turbineassembly (for example, a gas or wind turbine), and freezes on thesurface. The build-up of ice on aircraft, turbine components, and otherequipment exposed to the weather, increases safety risks and generatescosts for periodic ice removal operations. Certain embodiments of thepresent invention include an aircraft that comprises the articles andmaterials described above; a component of such an aircraft suitable toserve as the embodied article may include, for example, a wing, tail,fuselage, or an aircraft engine component. Non-limiting examples ofaircraft engine components that are suitable as articles in embodimentsof the present invention include the nacelle inlet lip, splitter leadingedge, booster inlet guide vanes, fan outlet guide vanes, sensors and/ortheir shields, and fan blades.

Icing is a significant problem for wind turbines, as the build-up of iceon various components such as anemometers and turbine blades reduces theefficiency and increases the safety risks of wind turbine operations.Wind turbine blades and other components are often made of lightweightcomposite materials such as fiberglass in order to save weight, and thebuild-up of ice can deleteriously load the blades to a point thatsignificantly reduces their effectiveness. In certain embodiments of thepresent invention, an article as described above is a component, such asa turbine blade, anemometer, gearbox, or other component, of a windturbine assembly.

As other components exposed to the weather are also adversely affectedby ice and/or water accumulation, other embodiments may include, forinstance, components of other items exposed to the weather, such aspower lines and antennas. The ability to resist wetting may benefit ahost of components that are so exposed, and the examples presentedherein should not be read as limiting embodiments of the presentinvention to only those named applications.

One particularly useful potential application for some of the materialsdescribed herein include applications involving the transmission ofelectromagnetic radiation, especially infrared (IR), visible, and/orultraviolet (UV) radiation. Those skilled in the art will appreciatethat many of the oxides described herein are made of components, such asytterbium oxide, for instance, that readily transmit radiation oversignificant portions of the visible and near visible (IR and UV)spectrum. Transparent oxides may be formed according to the methodsdescribed herein by controlling the composition and microstructure ofthe oxides. For example, where transparency is desired for a specifiedwavelength range, component oxides may be selected that do notsubstantially absorb in that range, and the material is then processedaccording to known methods to minimize defects that would scatterincident radiation. As an example, ytterbium oxide is transparent in thevisible spectrum, and the present inventors have demonstrated pureytterbium oxide coatings that are transparent to visible light and thatare hydrophobic. Coatings comprising ytterbium gadolinium oxides areanother example of hydrophobic materials that are also transparent overthe visible spectrum up to about 900 nanometer wavelengths. Thetransparent material may be disposed as a coating 102 on a substrate104, or may be a monolithic material. In particular embodiments of thearticles described previously, coating 102, or surface 200, asappropriate, comprises a material that is transparent to electromagneticradiation of at least one type selected from the group consisting ofultraviolet radiation, visible light, and infrared radiation. Inparticular embodiments, the substrate 104 comprises a material that isalso transparent to the radiation. One example of a potentially usefulapplication of the transparent material described above includesphotovoltaic devices. Another example is a window of any type. Here“window” embraces any component designed to allow at least some incidentvisible or near visible radiation to transmit; examples include, but arenot limited to, windows for buildings, windshields for vehicles, andcomponents of sensors designed to sense or emit certain wavelengths ofradiation. The hydrophobic and/or dropwise condensation-promotingproperties of the transparent materials described herein allow thepotential for windows and the like that easily shed dirt and water thatmay otherwise foul the surface and detract from performance.

EXAMPLES

Without further elaboration, it is believed that one skilled in the artcan, using the description herein, utilize the present invention to itsfullest extent. The following examples are included to provideadditional guidance to those skilled in the art in practicing theclaimed invention. The examples provided are merely representative ofthe work that contributes to the teaching of the present application.Accordingly, these examples are not intended to limit the invention, asdefined in the appended claims, in any manner.

Example 1:

A coating in accordance with embodiments described herein was depositedon an optically transparent quartz substrate by radio frequencymagnetron sputtering. The sputtering target was obtained commerciallyhaving a composition of Yb2O3 (99.9% pure). A coating with a thicknessof about 300 nm was produced using a deposition rate of about 100 Å/minat a forward power of 100 watts in a 7% oxygen/93% argon gas mixture.The contact angle with water for the coatings was about 93 degrees. Thecoating exhibited dropwise condensations in steam. The coating had atransparency of greater than 80% over the range of 250 to 2500 nm.

Example2:

Sintered oxide disks were formed of various oxides in accordance withembodiments described herein by combining two component oxides in apredetermined molar ratio and sintering in air at 1600 degrees Celsius.Contact angle measurements with water were measured, and some of thisdata is presented in FIG. 3 (Eu—Yb oxides), FIG. 4 (Eu—Gd oxides), FIG.5 (Yb—Gd oxides), and FIG. 6 (Yb—Nd oxides). All of the compositionswere tested in a condensation chamber at atmospheric pressure and theircharacteristics for promoting water condensation were evaluated. In eachinstance, the materials were found to promote drop-wise condensation.

While only certain features of the invention have been illustrated anddescribed herein, many modifications and changes will occur to thoseskilled in the art. It is, therefore, to be understood that the appendedclaims are intended to cover all such modifications and changes as fallwithin the true spirit of the invention.

1. A material comprising: an oxide comprising from about 60 mole % toabout 95 mole % gadolinia and at least about 1 mole % ytterbia oreuropia, wherein the oxide is B-type monoclinic and wherein the oxidehas up to about 25 atomic percent of its total cation content astetravalent cations.
 2. The material of claim 1, wherein the oxidecomprises up to about 30 mole percent ytterbia.
 3. The material of claim2, wherein the oxide comprises at least about 70 mole percent gadolinia.4. The material of claim 1, wherein the oxide comprises up to about 25mole percent europia.
 5. The material of claim 4, wherein the oxidecomprises at least about 75 mole percent gadolinia.
 6. The material ofclaim 4, wherein the oxide further comprises samaria, dysprosia, orterbia.
 7. The material of claim 1, wherein the oxide comprises ytterbiaand europia.
 8. The material of claim 7, wherein the total amount ofytterbia and europia present in the oxide is below about 40 mole %. 9.The material of claim 7, wherein the oxide further comprises samaria,dysprosia, or terbia.
 10. The material of claim 2, wherein the oxidecomprises x mole percent of ytterbia and 100-x mole percent ofgadolinia, wherein x is up to about 30 mole percent.
 11. The material ofclaim 2, wherein the oxide comprises x mole percent of europia and 100-xmole percent of gadolinia, wherein x is up to about 25 mole percent. 12.The material of claim 1, wherein the oxide is transparent toelectromagnetic radiation of at least one type selected from the groupconsisting of ultraviolet radiation, visible light, and infraredradiation.
 13. A material comprising: an oxide comprising at least about50 mole % europia; and samaria, terbia, or dysprosia; wherein thematerial contains up to about 25 atom % of tetravalent cations relativeto the total amount of cations present in the material.
 14. The materialof claim 13, wherein the oxide is B-type monoclinic.
 15. The material ofclaim 13, wherein the material consists essentially of the oxide.
 16. Amaterial comprising: a B-type monoclinic oxide comprising ytterbia andeuropia; wherein the oxide contains up to about 25 atom % of tetravalentcations relative to the total amount of cations present in the material.17. The material of claim 16, wherein the material consists essentiallyof ytterbia and europia.
 18. The material of claim 16, wherein the oxidefurther comprises an additional material selected from the groupconsisting of Sm, Tb, or Dy, wherein the total amount of said additionalmaterial is up to about 50 mole %.